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THE FIRST SUN (NATURE REPUBLIC CO., LTD.)

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LIQUID 40 mL in 1 CARTON (51346-001-01) Label Information

Complete THE FIRST SUN Information

  • Active Ingredient

    Active Ingredients:
    ETHYLHEXYL METHOXYCINNAMATE 7.5%, ZINC OXIDE 6.5%, ETHYLHEXYL SALICYLATE 5%, TITANIUM DIOXIDE 2.5%


  • Inactive Ingredient

    Inactive Ingredients:
    WATER, CYCLOPENTASILOXANE, ALCOHOL, DICAPRYLYL CARBONATE, BIOSACCHARIDE GUM-1, BUTYLENE GLYCOL, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, METHYL METHACRYLATE CROSSPOLYMER, PHENOXYETHANOL, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL, POLYGLYCERYL-6 POLYRICINOLEATE, SACCHAROMYCES FERMENT, OLEA EUROPAEA (OLIVE) FRUIT OIL, ACACIA SENEGAL FLOWER/STEM EXTRACT, CITRUS AURANTIFOLIA (LIME) OIL, RIBES NIGRUM (BLACK CURRANT) SEED OIL, ROSE FLOWER OIL, ILLICIUM VERUM (ANISE) FRUIT/SEED OIL, EUTERPE OLERACEA FRUIT EXTRACT, HYDROLYZED COLLAGEN, SODIUM LAUROYL SARCOSINATE, SOLUBLE COLLAGEN


  • Purpose

    Purpose: This sun liquid, with its active ingredients of fermented enzyme, makes your skin look clear and transparent.


  • WARNINGS

    Cautions:
    For external use only.
    Avoid contact with eyes and mouth.
    Discontinue use if signs of irritation or rash appear
    Replace the cap after use.


  • Keep out of reach of children

    Keep out of reach of children:

    Keep out of reach of children


  • INDICATION AND USAGE

    How to Use:
    Gently shake the bottle before use.
    Apply an appropriate amount to your face, following the skin's texture and softly pat your face
    to enhance its absorption into your skin.


  • DOSAGE AND ADMINISTRATION

    How to Use:
    Gently shake the bottle before use.
    Apply an appropriate amount to your face, following the skin's texture and softly pat your face
    to enhance its absorption into your skin.


  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

    Image of carton


  • INGREDIENTS AND APPEARANCE
    THE FIRST SUN  SPF50 PLUS PA PLUS PLUS PLUS
    octinoxate, zinc oxide, octisalate, titanium dioxide liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51346-001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3 g  in 40 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 2.61 g  in 40 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2 g  in 40 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 1 g  in 40 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51346-001-01 40 mL in 1 CARTON
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 03/01/2012
    Labeler - NATURE REPUBLIC CO., LTD. (631172020)
    Registrant - NATURE REPUBLIC CO., LTD. (631172020)
    Establishment
    Name Address ID/FEI Business Operations
    NATURE REPUBLIC CO., LTD. 631172020 manufacture(51346-001)